Supplemental material
Journal of Biomolecular Structure and Dynamics
Volume 35, 2017 - Issue 10
Reprints and Corporate Permissions
Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?
To request a reprint or corporate permissions for this article, please click on the relevant link below:
Academic Permissions
Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?
Obtain permissions instantly via Rightslink by clicking on the button below:
If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.
Related Research Data
HADDOCK: a protein-protein docking approach based on biochemical or biophysical information.
Source:
American Chemical Society (ACS)
Screening of the FUS gene in Chinese ALS cases
Source:
Wiley
Structural Basis for Substrate Recognition and Dissociation by Human Transportin 1
Source:
Elsevier BV
Sporadic juvenile amyotrophic lateral sclerosis caused by mutant FUS/TLS: possible association of mental retardation with this mutation
Source:
Springer Science and Business Media LLC
Computer-aided drug design platform using PyMOL
Source:
Springer Science and Business Media LLC
GROMACS 4: Algorithms for highly efficient, load-balanced, and scalable molecular simulation
Source:
American Chemical Society (ACS)
Structural and energetic basis of ALS-causing mutations in the atypical proline–tyrosine nuclear localization signal of the Fused in Sarcoma protein (FUS)
Source:
Proceedings of the National Academy of Sciences
Rules for Nuclear Localization Sequence Recognition by Karyopherinβ2
Source:
Elsevier BV
Arginine methylation by PRMT1 regulates nuclear-cytoplasmic localization and toxicity of FUS/TLS harbouring ALS-linked mutations
Source:
Oxford University Press (OUP)
FUS mutations in familial ALS
Source:
Wiley
Molecular dynamics and molecular docking studies on E166A point mutant, R274N/R276N double mutant, and E166A/R274N/R276N triple mutant forms of class A β-lactamases
Source:
Informa UK Limited
TDP-43 and FUS: a nuclear affair
Source:
Elsevier BV
Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia.
Source:
Ovid Technologies (Wolters Kluwer Health)
Recognition of nuclear targeting signals by Karyopherin-β proteins.
Source:
Elsevier BV
Novel FUS mutation in patients with sporadic amyotrophic lateral sclerosis and corticobasal degeneration
Source:
Elsevier BV
A Japanese ALS6 family with mutation R521C in the FUS/TLS gene: A clinical, pathological and genetic report ☆
Source:
Elsevier BV
Nuclear import by karyopherin-βs: recognition and inhibition.
Source:
Elsevier BV
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort
Source:
Ovid Technologies (Wolters Kluwer Health)
Lower motor neuron disease caused by a novel FUS/TLS gene frameshift mutation.
Source:
Springer Science and Business Media LLC
A smooth particle mesh Ewald method
Source:
AIP Publishing
Mutations in FUS cause FALS and SALS in French and French Canadian populations
Source:
Ovid Technologies (Wolters Kluwer Health)
Atomic resolution structures in nuclear transport
Source:
Elsevier BV
The Protein Data Bank.
Source:
International Union of Crystallography (IUCr)
Linking provided by
